Canonical Allele Identifier: CA2229310001
Gene: HSD11B2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.67436275G= , CM000678.2:g.67436275G= GRCh38
NC_000016.9:g.67470178G= , CM000678.1:g.67470178G= GRCh37
NC_000016.8:g.66027679G= NCBI36
NG_011482.1:g.49912C=
NG_016549.1:g.10143G=

Transcript Alleles

HGVS Amino-acid change
ENST00000326152.6:c.691G= MANE Select ENSP00000316786.5:p.Ala231=
ENST00000326152.5:c.691G= ENSP00000316786.5:p.Ala231=
NM_000196.3:c.691G= NP_000187.3:p.Ala231=
NM_000196.4:c.691G= MANE Select NP_000187.3:p.Ala231=